Neuropeptides modulate RANKL and OPG expression in human periodontal ligament cells

被引:5
作者
Nakao, Kayoko [1 ]
Goto, Tetsuya [2 ]
Gunjigake, Kaori [1 ]
Konoo, Tetsuro [3 ]
Kobayashi, Shigeru [2 ]
Yamaguchi, Kazunori [1 ]
机构
[1] Kyushu Dent Coll, Div Orofacial Funct & Orthodont, Kokurakita, Japan
[2] Kyushu Dent Coll, Div Anat Kyushu, Kokurakita Ku, Kitakyushu, Fukuoka 8038580, Japan
[3] Kyushu Dent Coll, Div Comprehens Dent, Kitakyushu, Fukuoka, Japan
关键词
Substance P; CGRP; RANKL; OPG; Periodontal ligament cell;
D O I
10.1016/j.odw.2007.03.004
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Neuropeptides, such as substance P (SP) and calcitonin gene-related peptide ( CGRP), may be associated with bone remodeling in response to mechanical stress during orthodontic tooth movement. To investigate this hypothesis, we examined the effects of neuropeptides on the expression of receptor activator of nuclear factor kB ligand (RANKL) and osteoprotegerin (OPG) in human periodontal ligament (PDL) cells under compression in vitro. PDL cells were subjected to compressive force (2.0 g/cm(2)) continuously in the presence or absence of SP or CGRP for 2-4 days. The expression of the SP receptor, neurokinin 1-receptor (NK1-R), in PDL cells was confirmed by RT-PCR and immunofluorescent staining. The effects of neuropeptides (SP and CGRP) on the expression of RANKL and OPG mRNA were determined using RTPCR. PDL cells constitutively expressed NK1-R on both the mRNA and protein levels. Compressive force decreased OPG mRNA expression and increased RANKL mRNA expression. In the presence of neuropeptides, the OPG level decreased synergistically with compression. Neuropeptides stimulated RANKL expression without compression, whereas they decreased RANKL mRNA expression with compression. These results indicate that PDL cell compression induces the up-regulation of RANKL and down-regulation of OPG, whereas neuropeptides suppress the RANKL expression induced by compression. Therefore, the neuropeptides SP and CGRP may modulate bone remodeling by PDL cells during orthodontic tooth movement. (C) 2007 Elsevier Ltd and the Japanese Orthodontic Society. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
相关论文
共 41 条
[1]   Substance P enhances the inhibition of osteoblastic cell differentiation induced by lipopolysaccharide from Porphyromonas gingivalis [J].
Azuma, H ;
Kido, J ;
Ikedo, D ;
Kataoka, M ;
Nagata, T .
JOURNAL OF PERIODONTOLOGY, 2004, 75 (07) :974-981
[2]   Effects of calcitonin, amylin, and calcitonin gene-related peptide on osteoclast development [J].
Cornish, J ;
Callon, KE ;
Bava, U ;
Kamona, SA ;
Cooper, GJS ;
Reid, IR .
BONE, 2001, 29 (02) :162-168
[3]  
DAVIDOVITCH Z, 1988, DENT CLIN N AM, V32, P411
[4]   NK1, NK2, NK3 and CGRP1 receptors identified in rat oral soft tissues, and in bone and dental hard tissue cells [J].
Fristad, I ;
Vandevska-Radunovic, V ;
Fjeld, K ;
Wimalawansa, SJ ;
Kvinnsland, IH .
CELL AND TISSUE RESEARCH, 2003, 311 (03) :383-391
[5]   Compressive force induces osteoblast apoptosis via caspase-8 [J].
Goga, Y ;
Chiba, M ;
Shimizu, Y ;
Mitani, H .
JOURNAL OF DENTAL RESEARCH, 2006, 85 (03) :240-244
[6]   Light- and electron-microscopic study of the distribution of axons containing substance P and the localization of neurokinin-1 receptor in bone [J].
Goto, T ;
Yamaza, T ;
Kido, MA ;
Tanaka, T .
CELL AND TISSUE RESEARCH, 1998, 293 (01) :87-93
[7]   Substance P stimulates late-stage rat osteoblastic bone formation through neurokinin-1 receptors [J].
Goto, T. ;
Nakao, K. ;
Gunjigake, K. K. ;
Kido, M. A. ;
Kobayashi, S. ;
Tanaka, T. .
NEUROPEPTIDES, 2007, 41 (01) :25-31
[8]   Substance P activates osteoclast formation and osteoclastic bone resorption through the neurokinin-1 receptor [J].
Goto, T ;
Yamaza, T ;
Kido, MA ;
Tanaka, T .
ACTA HISTOCHEMICA ET CYTOCHEMICA, 2001, 34 (01) :31-38
[9]  
Goto Tetsuya, 2001, Medical Electron Microscopy, V34, P77
[10]   Correlation between the appearance of neuropeptides in the rat trigeminal ganglion and reinnervation of the healing root socket after tooth extraction [J].
Gunjigake, Kaori K. ;
Goto, Tetsuya ;
Nakao, Kayoko ;
Konoo, Tetsuro ;
Kobayashi, Shigeru ;
Yamaguchi, Kazunori .
ACTA HISTOCHEMICA ET CYTOCHEMICA, 2006, 39 (03) :69-77